Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association studyMie Rizig, FI Ojini, Sara Bandrés‐Ciga et al.|The Lancet Neurology|2023Cited by 154
Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylationMikhail Kolmogorov, Benedict Paten, P. Carnevali et al.|Nature Methods|2023Cited by 143
Mitochondrial <i>UQCRC1</i> mutations cause autosomal dominant parkinsonism with polyneuropathyChin‐Hsien Lin, Ruey‐Meei Wu, Pei-I Tsai et al.|Brain|2020Cited by 77
Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylationMikhail Kolmogorov, Benedict Paten, Kimberley J. Billingsley et al.|bioRxiv (Cold Spring Harbor Laboratory)|2023Cited by 31
Genome-wide Association Identifies Novel Etiological Insights Associated with Parkinson’s Disease in African and African Admixed PopulationsMie Rizig, FI Ojini, Sara Bandrés‐Ciga et al.|medRxiv|2023Cited by 18